Analysis of the MRPL3, DNAJC13 and OFCC1 variants in Chinese Han patients with TS-CTD

Author:

Guo Yi,Deng Xiong,Zhang Jie,Su Linyan,Xu Hongbo,Luo Ziqiang,Deng Hao

Publisher

Elsevier BV

Subject

General Neuroscience

Reference27 articles.

1. Sequence variants in SLITRK1 are associated with Tourette's syndrome;Abelson;Science,2005

2. Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome;Belloso;European Journal of Human Genetics,2007

3. Tourette syndrome in a pedigree with a 7;18 translocation: identification of a YAC spanning the translocation breakpoint at 18q22.3;Boghosian-Sell;American Journal of Human Genetics,1996

4. Tourette syndrome and klippel-feil anomaly in a child with chromosome 22q11 duplication;Clarke;Case Report Medicine,2009

5. Candidate locus for Gilles de la Tourette syndrome/obsessive compulsive disorder/chronic tic disorder at 18q22;Cuker;American Journal of Medical Genetics Part A,2004

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